Variants linked to Celiac Disease

Continuously updated · newest added Oct 25, 2026

20,582 positions on this site are linked to Celiac Disease, out of 117,648 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

← Back to Celiac Disease

Standard

FLT4 protein levels

near RNF130 · rs76993498

See detailed info →
Standard

WFDC12 protein levels

near RPS15AP27 · rs75795606

See detailed info →
Standard

BID protein levels

CFI · rs74817407

See detailed info →
Standard

CLEC4A protein levels

ZNF467 · rs73725601

See detailed info →
Standard

IL1RAP protein levels

near TMEM207 · rs73192474

See detailed info →
Standard

COL28A1 protein levels

COL28A1 · rs73038788

See detailed info →
Standard

SUSD5 protein levels

CRTAP · rs72859106

See detailed info →
Standard

Urate levels (UKB data field 30880)

near CPEB4 · rs67909753

See detailed info →
Standard

CDSN protein levels

PRUNE1 · rs6673178

See detailed info →
Standard

SCG3 protein levels

ARPP19 · rs62023330

See detailed info →
Standard

GLB1 protein levels

near IGF1 · rs61937480

See detailed info →
Standard

SERPING1 protein levels

near NOX4P1 · rs61885288

See detailed info →
Standard

Red blood cell erythrocyte distribution width (UKB data field 30070)

near H2AC2P · rs567942228

See detailed info →
Standard

PCSK9 protein levels

near RPSAP20 · rs565120608

See detailed info →
Standard

CA5A protein levels

JPH3 · rs560598297

See detailed info →
Standard

DYNLT1 protein levels

SMYD3 · rs552900551

See detailed info →
Standard

GLIPR1 protein levels

LINC02917 · rs546665931

See detailed info →
Standard

GLIPR1 protein levels

near NSG2 · rs543262238

See detailed info →
Standard

GLIPR1 protein levels

near RN7SKP211 · rs530132025

See detailed info →
Standard

GLIPR1 protein levels

ITGAM · rs529106699

See detailed info →

Showing 20 of 20582 · page 133 of 1030

Questions about variants on this site

What is a "variant" page on this site?

One specific position in the genome (an rsID), explained in plain language with what published research has found it linked to, and how strong that link actually is.

Where does new variant data come from?

The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.

Does being listed here mean a variant causes a condition?

No. Listing reflects an association from published research, not a diagnosis or a cause. Most common variants shift probability modestly rather than determining an outcome.

Can I search this list by gene or rsID?

Yes — the search box above matches gene symbols and rsIDs as well as trait names.